Abstract
Background: Our objective was to determine whether anti-interleukin (IL)-6 receptors improve outcomes of critically ill patients with coronavirus disease 2019 (COVID-19) pneumonia. We report on two cohort-embedded, investigator-initiated, multicentre, open-label, Bayesian randomised controlled clinical trials.
Methods: Patients were randomly assigned to receive either usual care (UC) or UC+tocilizumab (TCZ) 8 mg·kg -1 (TOCI-2 trial) or UC or UC+sarilumab (SARI) 200 mg (SARI-2 trial), both intravenously on day 1 and, if clinically indicated, on day 3.
Results: Between 31 March and 20 April 2020, 97 patients were randomised in the TOCI-2 trial, to receive UC (n=46) or UC+TCZ (n=51). At day 14, numbers of patients who did not need noninvasive ventilation (NIV) or mechanical ventilation (MV) and were alive with TCZ or UC were similar (47% versus 42%; median posterior hazard ratio (HR) 1.19, 90% credible interval (CrI) 0.71-2.04), with a posterior probability of HR >1 of 71.4%. Between 27 March and 4 April 2020, 91 patients were randomised in the SARI-2 trial, to receive UC (n=41) or UC+SARI (n=50). At day 14, numbers of patients who did not need NIV or MV and were alive with SARI or UC were similar (38% versus 33%; median posterior HR 1.05, 90% CrI 0.55-2.07), with a posterior probability of HR >1 of 54.9%. Overall, the risk of death up to day 90 was: UC+TCZ 24% versus UC 30% (HR 0.67, 95% CI 0.30-1.49) and UC+SARI 29% versus UC 39% (HR 0.74, 95% CI 0.35-1.58). Both TCZ and SARI increased serious infectious events.
Conclusion: In critically ill patients with COVID-19, anti-IL-6 receptors did not significantly increase the number of patients alive without any NIV or MV by day 14.
【초록키워드】 COVID-19, coronavirus disease, Coronavirus disease 2019, Bayesian, Trial, Open-label, randomised, mechanical ventilation, Tocilizumab, Pneumonia, sarilumab, Noninvasive ventilation, clinical trials, outcome, Critically ill, Patient, multicentre, receptor, critically ill patients, credible interval, not need, Critically ill patient, risk of death, 95% CI, usual care, hazard ratio, controlled clinical trials, posterior probability, SARI, intravenously, NIV, Randomly, TOCI, IMPROVE, significantly, indicated, clinically, events, median, determine, assigned, receive, anti-IL-6 receptor, CrI, investigator-initiated, numbers of patient, randomised controlled, TCZ, with COVID-19, 【제목키워드】 randomised controlled trial, group, interleukin-6 receptor, antagonist, Effect, patients with COVID-19,